NovoLet® Acceptance Study Within the Hospital Practise in Indonesia
NCT ID: NCT01492205
Last Updated: 2016-10-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
203 participants
OBSERVATIONAL
2005-09-30
2006-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Human insulin
insulin human
All subjects were treated with human insulin administered either by using the NovoLet® pre-filled insulin system or the conventional vial and syringe method. Doctors and nurses must personally administer at least 10 insulin doses to each patient under their individual clinical supervision for assessment of the NovoLet® pre-filled insulin system
Interventions
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insulin human
All subjects were treated with human insulin administered either by using the NovoLet® pre-filled insulin system or the conventional vial and syringe method. Doctors and nurses must personally administer at least 10 insulin doses to each patient under their individual clinical supervision for assessment of the NovoLet® pre-filled insulin system
Eligibility Criteria
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Inclusion Criteria
* Type 2 diabetes
* Likely to be hospitalised and require insulin therapy
18 Years
ALL
No
Sponsors
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Novo Nordisk A/S
INDUSTRY
Responsible Party
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Principal Investigators
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Global Clinical Registry (GCR, 1452)
Role: STUDY_DIRECTOR
Novo Nordisk A/S
Locations
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Novo Nordisk Investigational Site
Jakarta, , Indonesia
Countries
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Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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NOPEN3-1887
Identifier Type: -
Identifier Source: org_study_id
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